HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018019Generated: October 30, 2026
Dimethylformamide → 2-Chloro-5-methylpyridine-3-carbaldehyde
https://huagongshe.com/reaction/1018019
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diphosgene | HCID 10426 | — |
| Reactant | N-benzyl-N-(1-Propenyl)acetamide | HCID 53742793 | — |
| Product | 2-Chloro-5-methylpyridine-3-carbaldehyde | HCID 9834018 | 93.4% |
Reaction Steps
Dimethylformamide (13.54 g, 0.185 moles) was added to a well stirred and cooled material of diphosgene (36.64 g, 0.185 moles) at 4° C. in 30 minutes in an ice bath followed by N-benzyl-N-(1-Propenyl)acetamide (5 g, 0.026 moles) at the same temperature. The reaction mixture was further continued for 2 hours at 25° C. The ice cold bath was removed and heated to 75° C. for 5 hours. The orange-yellow coloured organic mass was poured in ice cold water (200 g) with stirring. The mass was extracted with methylenechloride (2×200 ml) and the layer was separated. The organic layer was dried over sodium sulfate, and the solvent was removed under reduced pressure. The obtained residue was subjected to chromatographic purification on silica gel to give 2-chloro-5-methylpyridine-3-carbaldehyde (3.78 g) in 92% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06479664B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-2a7457bb66b94277abdbfd10b6aaffe4 |
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| Source note | uspto-grants-2002_11 |
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